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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02045355
Other study ID # 2013/2004-WP4
Secondary ID
Status Terminated
Phase N/A
First received January 17, 2014
Last updated December 11, 2015
Start date February 2014
Est. completion date January 2017

Study information

Verified date December 2015
Source University of Bergen
Contact n/a
Is FDA regulated No
Health authority Norway: Data Protection AuthorityNorway: Directorate of HealthNorway: Ministry of Health and Care ServicesNorway: Norwegian Social Science Data Services
Study type Interventional

Clinical Trial Summary

Health effects of fish consumption have been demonstrated in epidemiological studies and in controlled intervention studies in a number of different population groups, however, randomized controlled studies on the effect of fish consumption in elderly are sparse. Many studies have focused on n-3 fatty acids instead of fish as a food and therefore, many health effects have only been related to the effect of n- 3 fatty acids. The elderly are a heterogeneous population group and therefore difficult to study. In order to reduce heterogeneity, it is advisable to focus on elderly with specific needs. Elderly who experienced a hip fracture can serve as a model for an advanced ageing process, as these patients typically experience a huge inflammatory response, immobilisation and a reduction in muscle mass. Increased fish intake is believed to have effects towards inflammation and a reduction in muscle mass. Therefore, we want to test whether increased fish intake can have positive health effects in elderly who experienced a hip fracture.

Main hypothesis:

Increased fish intake (salmon, cod, pelagic fish), in comparison to meat, will increase mobility, muscle strength and mobility in frail elderly.

Objectives

1. To evaluate the health effects of fish consumption in frail elderly The effect of a dietary intervention with fish on mobility, muscle mass and strength in elderly who experienced a hip fracture has not been shown before.

2. To demonstrate the feasibility of dietary intervention in elderly We want to show that a dietary intervention with fish or control meals is feasible in elderly. The meals (4 portions of fish per week or control portions of meat) will be delivered to their homes.

Description of work and role of participants This is a randomized clinical trial (RCT) on the effect of fish consumption on mobility in elderly who experienced a hip fracture. Elderly who experienced a hip fracture but were able to walk without support by a person before the fracture, will receive, after being randomized to two groups, fish or meat to be used in cold or warm meals at 4 days per week for a period of 16 weeks. Measurements will be taken at baseline (when patients have left the rehabilitation center), after 4 weeks and after 16 weeks. Measurements at 4 and 16 weeks after inclusion will be at their homes or in the outpatient clinic.


Recruitment information / eligibility

Status Terminated
Enrollment 14
Est. completion date January 2017
Est. primary completion date January 2016
Accepts healthy volunteers No
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

- Patients >65 years with a first hip fracture who have a reasonable high chance of returning to their homes after rehabilitation,

- with a sufficient cognitive function to understand the objectives of the study

- the ability to go / walk without support of a person prior to the hip fracture.

- the life expectancy should be more than 6 months.

- the ability to use the provided food and willingness to participate

- sign the informed consent.

Exclusion Criteria:

- Patients are excluded who will probably not return to their home but to a nursing home.

- Patients who lack the cognitive function to understand the study objectives

- Patients with a missing informed consent

- Patients with reduced life expectancy of less than 6 months.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
Fish intervention
The intervention will compare fish intake with a correspondent amount of meat. The basis for the comparison will be the estimated protein intake from fish and meat and should be almost similar both from fish and from meat. To ensure compliance and to add more variety to the diet, different fish types will be included in the intervention group and different meat sources in the control group. The types of fish (and that of meat in the control diet) that will be used will be accurately documented and will be similar for all participants included.

Locations

Country Name City State
Norway Haraldsplass Deacon Hospital Bergen Hordaland
Norway Haukeland University Hospital Bergen Hordaland

Sponsors (2)

Lead Sponsor Collaborator
University of Bergen The Research Council of Norway

Country where clinical trial is conducted

Norway, 

References & Publications (1)

Parker MJ, Palmer CR. A new mobility score for predicting mortality after hip fracture. J Bone Joint Surg Br. 1993 Sep;75(5):797-8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Change in inflammation Measurement of C-reactive protein in blood samples Baseline and 16 weeks No
Other Change of dietary habits Assessment of dietary habits using 24 hour recall. Baseline and 16 weeks No
Other Number of falls during intervention period Weekly assessment of falls in the previous week by questionnaires 16 weeks No
Primary Change in New Mobility Score (NMS) The NMS is an easy, reliable tool for the assessment of mobility. It is based on three questions, which are scored with 0 to 3, thus the result will be between 0 and 9 points. Baseline and 16 weeks No
Secondary Change of muscle mass Measure muscle mass by using Bioelectrical impedance (BIA Anniversary 100) Baseline and 16 weeks No
Secondary Change in Vitamin D status Measurement of serum 25OHD. Baseline and 16 weeks No
Secondary Change of muscle strength Hand grip measurement (JAMAR). Baseline and 16 weeks No
Secondary Change of self-perceived health Standardized questionnaire (EuroQol 5D) Recruitment and 4 months No
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